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可编程起搏器的临床经验。

Clinical experience with a programmable pacemaker.

作者信息

Venkataraman K, Bilitch M

出版信息

Pacing Clin Electrophysiol. 1980 Sep;3(5):605-11. doi: 10.1111/j.1540-8159.1980.tb05281.x.

Abstract

As part of a study to evaluate a new programmable pacemaker, 15 patients received lithium-powered R-wave inhibited, unipolar pulse-generators (CPI Model 0505). Five were initial implants (Group I) and 10 were pulse generator replacements (Group II). The follow-up period ranged from 1 to 18 months (mean 11 months). There were 5 deaths unrelated to the pacemaker. Three instances of pacemaker failure were identified and were characterized by a sudden loss of pacemaker output. THe malfunction, traced to a 10 kHz timing crystal, has been corrected in subsequently manufactured pulse-generators. In 11 patients, the pacemakers were programmed at a pulse width which was twice the threshold determined at 3 months. Four were programmed at 0.1 ms, three at 0.2 ms and four at 0.4 ms. Although no complications were seen in patients programmed at 0.1 ms pulse width, it might be advisable to leave pacemakers at 0.2 ms or greater for chronic pacing in patients with a pulse width threshold at 0.05 mg.

摘要

作为评估新型程控起搏器研究的一部分,15名患者接受了锂供电的R波抑制型单极脉冲发生器(CPI 0505型)。其中5名是初次植入(第一组),10名是脉冲发生器更换(第二组)。随访期为1至18个月(平均11个月)。有5例死亡与起搏器无关。发现3例起搏器故障,其特征为起搏器输出突然丧失。故障追溯到一个10 kHz定时晶体,在随后生产的脉冲发生器中已得到纠正。11名患者的起搏器被程控为脉冲宽度是3个月时测定阈值的两倍。4名患者程控为0.1 ms,3名患者程控为0.2 ms,4名患者程控为0.4 ms。尽管在程控为0.1 ms脉冲宽度的患者中未观察到并发症,但对于脉冲宽度阈值为0.05 mg的患者,长期起搏时将起搏器程控为0.2 ms或更宽可能更为合适。

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